A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012702



Internal ID19101919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:198062049..198129562hg38UCSC Ensembl
Innerchr3:197788920..197856433hg19UCSC Ensembl
Innerchr3:199273317..199340830hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3867514
hg1967514
hg1867514
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3617042
Samples
Known GenesANKRD18DP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1012702
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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